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06720

Sigma-Aldrich

2-Aminoethyl hydrogen sulfate

≥98.0% (T)

Synonym(s):

Sulfuric acid mono 2-aminoethylester

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About This Item

Linear Formula:
NH2CH2CH2OSO3H
CAS Number:
926-39-6
Molecular Weight:
141.15
Beilstein:
1704079
EC Number:
213-135-7
MDL number:
MFCD00008179
UNSPSC Code:
12352100
PubChem Substance ID:
24845962
NACRES:
NA.22

Assay

≥98.0% (T)

mp

277 °C (dec.) (lit.)

SMILES string

NCCOS(O)(=O)=O

InChI

1S/C2H7NO4S/c3-1-2-7-8(4,5)6/h1-3H2,(H,4,5,6)

InChI key

WSYUEVRAMDSJKL-UHFFFAOYSA-N

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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D V Coscina et al.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity, 16(6), 425-433 (1992-06-01)
To explore recent suggestions that genetically obese Zucker rats show less anorexia when brain gamma-aminobutyric acid (GABA) is elevated, obese vs. lean littermates received 100, 50 and 0 micrograms of the GABA-transaminase inhibitor, ethanolamine-O-sulfate (EOS), intra-cisternally in a longitudinal design
GABA-mimetic compounds block haloperidol-induced hyperprolactinemia in rats.
L Debeljuk et al.
Advances in biochemical psychopharmacology, 42, 139-144 (1986-01-01)
Célia M C Faustino et al.
The journal of physical chemistry. B, 113(4), 977-982 (2009-01-23)
New anionic urea-based surfactants derived from alpha,omega-amino acids and in particular from beta-alanine were synthesized and their solution properties characterized by electrical conductivity, equilibrium surface tension, and steady-state fluorescence spectroscopy techniques. Double-chain surfactants and the single-chain surfactant containing a sulfate
J P Loeffler et al.
Neuroendocrinology, 43(4), 504-510 (1986-01-01)
The inhibitory action of gamma-aminobutyric acid (GABA) on prolactin (PRL) messenger ribonucleic acid (mRNA) levels was studied in vitro in rat anterior pituitary cells in culture and in intact rats in vivo. PRL mRNA levels were determined by hybridization of
M Qume et al.
Biochemical pharmacology, 52(9), 1355-1363 (1996-11-08)
The inhibitory neurotransmitter gamma-aminobutyric acid (GABA) is not solely located in the CNS, it and the enzymes responsible for its synthesis (glutamic acid decarboxylase, GAD, EC 4.1.1.15) and catabolism (GABA-transaminase, GABA-T, EC 2.6.1.19) are also present in non-neuronal organs. Following
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